Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10132898	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10134005	0.95[ASN][1000 genomes]
rs10145673	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10148642	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10150745	0.95[ASN][1000 genomes]
rs12436486	0.91[EUR][1000 genomes]
rs17707121	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28399118	0.96[ASN][1000 genomes]
rs28446157	0.96[ASN][1000 genomes]
rs3924602	0.92[EUR][1000 genomes]
rs3935697	0.96[ASN][1000 genomes]
rs4277275	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4372623	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55986944	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7142508	0.95[ASN][1000 genomes]
rs7143199	0.95[ASN][1000 genomes]
rs7154367	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7157365	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7157373	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8005901	0.96[ASN][1000 genomes]
rs8009583	0.96[ASN][1000 genomes]
rs8012329	0.95[ASN][1000 genomes]
rs8019836	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902161	chr14:84699866-84769903	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84765400-84769600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:84766000-84768400	Weak transcription	Adipose Nuclei	Adipose
3	chr14:84766000-84769000	Weak transcription	Esophagus	oesophagus
4	chr14:84768200-84768600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:84768200-84768800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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